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Self-Assembled DNA Immunonanoflowers as Multivalent CpG Nanoagents

[Image: see text] Synthetic unmethylated cytosine–guanine (CpG) oligodeoxynucleotides are immunostimulatory motifs that have shown promise as vaccines or adjuvants for diseases such as cancers and infectious diseases. In the present work, novel immuno-nanoflowers (NFs), self-assembled from long DNA...

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Autores principales: Zhang, Liqin, Zhu, Guizhi, Mei, Lei, Wu, Cuichen, Qiu, Liping, Cui, Cheng, Liu, Yuan, Teng, I-Ting, Tan, Weihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898273/
https://www.ncbi.nlm.nih.gov/pubmed/26440045
http://dx.doi.org/10.1021/acsami.5b06987
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author Zhang, Liqin
Zhu, Guizhi
Mei, Lei
Wu, Cuichen
Qiu, Liping
Cui, Cheng
Liu, Yuan
Teng, I-Ting
Tan, Weihong
author_facet Zhang, Liqin
Zhu, Guizhi
Mei, Lei
Wu, Cuichen
Qiu, Liping
Cui, Cheng
Liu, Yuan
Teng, I-Ting
Tan, Weihong
author_sort Zhang, Liqin
collection PubMed
description [Image: see text] Synthetic unmethylated cytosine–guanine (CpG) oligodeoxynucleotides are immunostimulatory motifs that have shown promise as vaccines or adjuvants for diseases such as cancers and infectious diseases. In the present work, novel immuno-nanoflowers (NFs), self-assembled from long DNA integrated with tandem CpG through rolling circle replication, were developed for efficient CpG delivery and protection from nuclease degradation. In a model of macrophage-like cells, the CpG NFs proved to be potent immunostimulators by triggering the proliferation of these immune cells, which, in turn, secreted immunostimulatory cytokines, including tumor necrosis factor α, interleukin-6, and interleukin-10. These results demonstrate the ability of CpG NFs to induce cancer cell apoptosis and necrosis.
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spelling pubmed-48982732016-10-06 Self-Assembled DNA Immunonanoflowers as Multivalent CpG Nanoagents Zhang, Liqin Zhu, Guizhi Mei, Lei Wu, Cuichen Qiu, Liping Cui, Cheng Liu, Yuan Teng, I-Ting Tan, Weihong ACS Appl Mater Interfaces [Image: see text] Synthetic unmethylated cytosine–guanine (CpG) oligodeoxynucleotides are immunostimulatory motifs that have shown promise as vaccines or adjuvants for diseases such as cancers and infectious diseases. In the present work, novel immuno-nanoflowers (NFs), self-assembled from long DNA integrated with tandem CpG through rolling circle replication, were developed for efficient CpG delivery and protection from nuclease degradation. In a model of macrophage-like cells, the CpG NFs proved to be potent immunostimulators by triggering the proliferation of these immune cells, which, in turn, secreted immunostimulatory cytokines, including tumor necrosis factor α, interleukin-6, and interleukin-10. These results demonstrate the ability of CpG NFs to induce cancer cell apoptosis and necrosis. American Chemical Society 2015-10-06 2015-11-04 /pmc/articles/PMC4898273/ /pubmed/26440045 http://dx.doi.org/10.1021/acsami.5b06987 Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Zhang, Liqin
Zhu, Guizhi
Mei, Lei
Wu, Cuichen
Qiu, Liping
Cui, Cheng
Liu, Yuan
Teng, I-Ting
Tan, Weihong
Self-Assembled DNA Immunonanoflowers as Multivalent CpG Nanoagents
title Self-Assembled DNA Immunonanoflowers as Multivalent CpG Nanoagents
title_full Self-Assembled DNA Immunonanoflowers as Multivalent CpG Nanoagents
title_fullStr Self-Assembled DNA Immunonanoflowers as Multivalent CpG Nanoagents
title_full_unstemmed Self-Assembled DNA Immunonanoflowers as Multivalent CpG Nanoagents
title_short Self-Assembled DNA Immunonanoflowers as Multivalent CpG Nanoagents
title_sort self-assembled dna immunonanoflowers as multivalent cpg nanoagents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898273/
https://www.ncbi.nlm.nih.gov/pubmed/26440045
http://dx.doi.org/10.1021/acsami.5b06987
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